calcium acetate
Generic: calcium acetate
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
calcium acetate
Generic Name
calcium acetate
Labeler
rising pharma holdings, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
calcium acetate 667 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
16571-813
Product ID
16571-813_f2fd0134-44cd-4d74-835f-980de3e5d9c0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211038
Listing Expiration
2026-12-31
Marketing Start
2021-11-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16571813
Hyphenated Format
16571-813
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
calcium acetate (source: ndc)
Generic Name
calcium acetate (source: ndc)
Application Number
ANDA211038 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 667 mg/1
Packaging
- 200 CAPSULE in 1 BOTTLE, PLASTIC (16571-813-20)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f2fd0134-44cd-4d74-835f-980de3e5d9c0", "openfda": {"unii": ["Y882YXF34X"], "rxcui": ["359296"], "spl_set_id": ["ce650ba5-fb42-e444-e053-2a95a90a075a"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 CAPSULE in 1 BOTTLE, PLASTIC (16571-813-20)", "package_ndc": "16571-813-20", "marketing_start_date": "20211101"}], "brand_name": "Calcium Acetate", "product_id": "16571-813_f2fd0134-44cd-4d74-835f-980de3e5d9c0", "dosage_form": "CAPSULE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "16571-813", "generic_name": "Calcium Acetate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Calcium Acetate", "active_ingredients": [{"name": "CALCIUM ACETATE", "strength": "667 mg/1"}], "application_number": "ANDA211038", "marketing_category": "ANDA", "marketing_start_date": "20211101", "listing_expiration_date": "20261231"}